Featured Articles

  1. Gain Insights And Speed With Remote Monitoring Of Equipment 3/10/2026

    Real-time equipment insights are reshaping how biopharma teams maintain uptime. See how data-driven oversight enables faster responses, smarter decisions, and more resilient operations.

  2. Can Your Biopharma Team Keep Unplanned Downtime At Bay? 3/10/2026

    Learn how teams reduce downtime, strengthen compliance, and respond quickly to equipment issues through proactive maintenance, smart spare parts planning, and digital troubleshooting tools.

  3. Stay cGMP Compliant: Instrument Requalification In Pharma 3/10/2026

    Maintaining equipment is an ongoing GxP requirement. Learn what triggers requalification, why it matters for operational continuity, and how proactive evaluation helps prevent costly disruptions.

  4. Comparing Process Development Approaches For Recombinant Proteins 2/26/2026

    Explore how adding a traceless tag enables streamlined affinity purification for recombinant proteins, and how this approach compares with a conventional process in development time, recovery, and purity.

  5. Host Cell Protein (HCP) Removal Post Virus Inactivation In mAb Processing 2/26/2026

    Clarifying post–virus inactivation streams with a charged depth filter can remove precipitates while significantly reducing HCPs. See how a dual‑layer filtration approach supports stronger impurity control.

  6. If Sustainability Is A Priority, Why Is Progress So Slow? 2/10/2026

    Sustainability is now central to biopharma strategy. New data reveals why commitments aren’t translating into action, and the roadblocks leaders must address to turn environmental ambition into change.

  7. New Year, New Biopharma: Game Changers We're Betting On 1/15/2026

    Digital innovation and regulatory evolution are reshaping biopharma. From AI to breakthroughs in oncology and gene editing, discover the trends and challenges that could define the industry.

  8. Sterile Injectables: Why Innovation Matters More Than Ever 1/15/2026

    New technologies and regulatory changes are shaping safer, more efficient filling processes. Discover why innovation is key to protecting patients and advancing therapies.

  9. Three Tips To Put Your Viral Vector On The Path To Regulatory Success 1/15/2026

    Gene therapy regulations are evolving fast, creating uncertainty for developers. Discover three strategies to navigate approval challenges and keep pace with changing expectations.

  10. Wetting Recommendations For Successful Filter Integrity Testing 1/12/2026

    Discover best practices for hydrophobic and hydrophilic filters, troubleshoot failures, and optimize wetting in stainless steel and single-use systems to ensure process reliability and product quality.